The goal of this proposal is to gain insight into the molecular processes controlling alternate ab/gd lineage commitment. This is of critical importance not only because the divergence of T cells into functionally distinct ab and gd lineages is essential for normal immune responses, but also because differentiation of multipotential precursor cells into distinct cell types is a fundamental yet poorly understood process common to all multicellular organisms. Despite much effort, relatively little insight has been gained into the developmental cues that determine whether an immature thymocyte will adopt the ab or gd lineage. Importantly, we recently provided compelling evidence for a signal strength model of lineage commitment which posits that weak signals promote commitment to the ab lineage while comparatively strong signals promote commitment to the gd lineage, irrespective of the TCR complex from which they originate. In pursuing these studies, we exploited an ideally suited gd-TCR transgenic model (KN6), which has a known ligand whose expression can be manipulated to alter the nature of the resultant TCR signal. We have demonstrated that the KN6 gd TCR complex requires engagement by ligands to promote adoption of the gd fate. This finding was highly controversial when first reported, but is now gaining support as other TCR/ligand pairs are examined. We further proposed that the differences in signal strength that alter fate are dependent upon differential activation of the ERK-early growth response (Egr)-Id3 pathway. In the current proposal, key features of the signal strength model will be tested as follows.
In Aim 1, we will assess the affinity of the selecting ligands, as well as whether they regulate fate instructively. Based on our observation that differential activation of ERK influences fate determination, Aim 2 is focused on investigating the importance of the amplitude and duration of ERK activation on commitment. In particular, we will investigate the function of ERK DEF domains, a key domain in mediating the effects of a long ERK signal. Finally, we have shown that Id3 is a downstream target of strong signals that promotes the gd fate and antagonizes the ab fate in our KN6 model, in addition to perturbing the development of gd lineage cells in non-Tg Id3-deficient mice. Hence, in Aim 3, we will elucidate the molecular mechanism whereby Id3 regulates gd T cell development. Our investigation of molecular effectors controlling T lineage commitment is of fundamental importance not only for thymocyte development, but also for other developmental processes, since control of cell growth and differentiation is a recurring theme in development and transformation.

Public Health Relevance

gd T cells regulate inflammation, preserve the integrity of epithelial barriers, and have been shown to be particularly adept at killing cutaneous tumors. Accordingly, understanding how their generation in the thymus is regulated may enable manipulation of their production for therapeutic benefit.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI081314-09
Application #
8289519
Study Section
Special Emphasis Panel (ZRG1-IMM-J (02))
Program Officer
Prabhudas, Mercy R
Project Start
2009-07-01
Project End
2014-06-30
Budget Start
2012-07-01
Budget End
2013-06-30
Support Year
9
Fiscal Year
2012
Total Cost
$427,569
Indirect Cost
$182,544
Name
Research Institute of Fox Chase Cancer Center
Department
Type
DUNS #
064367329
City
Philadelphia
State
PA
Country
United States
Zip Code
19111
Lee, Sang-Yun; Coffey, Francis; Fahl, Shawn P et al. (2014) Noncanonical mode of ERK action controls alternative ?? and ?? T cell lineage fates. Immunity 41:934-46
Coffey, Francis; Lee, Sang-Yun; Buus, Terkild B et al. (2014) The TCR ligand-inducible expression of CD73 marks ?? lineage commitment and a metastable intermediate in effector specification. J Exp Med 211:329-43
Dutta, Mala; Kraus, Zachary J; Gomez-Rodriguez, Julio et al. (2013) A role for Ly108 in the induction of promyelocytic zinc finger transcription factor in developing thymocytes. J Immunol 190:2121-8
del Blanco, Beatriz; Garcia-Mariscal, Alberto; Wiest, David L et al. (2012) Tcra enhancer activation by inducible transcription factors downstream of pre-TCR signaling. J Immunol 188:3278-93
Lee, Sang-Yun; Stadanlick, Jason; Kappes, Dietmar J et al. (2010) Towards a molecular understanding of the differential signals regulating alphabeta/gammadelta T lineage choice. Semin Immunol 22:237-46
Park, Kyewon; He, Xi; Lee, Hyung-Ok et al. (2010) TCR-mediated ThPOK induction promotes development of mature (CD24-) gammadelta thymocytes. EMBO J 29:2329-41
Lauritsen, Jens Peter Holst; Wong, Gladys W; Lee, Sang-Yun et al. (2009) Marked induction of the helix-loop-helix protein Id3 promotes the gammadelta T cell fate and renders their functional maturation Notch independent. Immunity 31:565-75